A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12188372



Internal ID6789191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10352508..10356808hg38UCSC Ensembl
Innerchr6:10352508..10356808hg38UCSC Ensembl
Outerchr6:10352193..10356827hg38UCSC Ensembl
chr6:10352741..10357041hg19UCSC Ensembl
Innerchr6:10352741..10357041hg19UCSC Ensembl
Outerchr6:10352426..10357060hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg384301
hg194301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3608070
Supporting Variants
SamplesNA20885
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12188372
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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